Functional Magnetic Core-Shell System-Based Iron Oxide Nanoparticle Coated with Biocompatible Copolymer for Anticancer Drug Delivery

Polymer coating has drawn increasing attention as a leading strategy to overcome the drawbacks of superparamagnetic iron oxide nanoparticles (SPIONs) in targeted delivery of anticancer drugs. In this study, SPIONs were modified with heparin-Poloxamer (HP) shell to form a SPION@HP core-shell system f...

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Main Authors: Thai Thanh Hoang Thi (Author), Diem-Huong Nguyen Tran (Author), Long Giang Bach (Author), Hieu Vu-Quang (Author), Duy Chinh Nguyen (Author), Ki Dong Park (Author), Dai Hai Nguyen (Author)
Format: Book
Published: MDPI AG, 2019-03-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Thai Thanh Hoang Thi  |e author 
700 1 0 |a Diem-Huong Nguyen Tran  |e author 
700 1 0 |a Long Giang Bach  |e author 
700 1 0 |a Hieu Vu-Quang  |e author 
700 1 0 |a Duy Chinh Nguyen  |e author 
700 1 0 |a Ki Dong Park  |e author 
700 1 0 |a Dai Hai Nguyen  |e author 
245 0 0 |a Functional Magnetic Core-Shell System-Based Iron Oxide Nanoparticle Coated with Biocompatible Copolymer for Anticancer Drug Delivery 
260 |b MDPI AG,   |c 2019-03-01T00:00:00Z. 
500 |a 1999-4923 
500 |a 10.3390/pharmaceutics11030120 
520 |a Polymer coating has drawn increasing attention as a leading strategy to overcome the drawbacks of superparamagnetic iron oxide nanoparticles (SPIONs) in targeted delivery of anticancer drugs. In this study, SPIONs were modified with heparin-Poloxamer (HP) shell to form a SPION@HP core-shell system for anticancer drug delivery. The obtained formulation was characterized by techniques including transmission electron microscopy (TEM), Fourier transform infrared spectra (FT-IR), vibration sample magnetometer (VSM), proton nuclear magnetic resonance (1H-NMR), and powder X-ray diffraction (XRD). Results showed the successful attachment of HP shell on the surface of SPION core and the inability to cause considerable effects to the crystal structure and unique magnetic nature of SPION. The core-shell system maintains the morphological features of SPIONs and the desired size range. Notably, Doxorubicin (DOX), an anticancer drug, was effectively entrapped into the polymeric shell of SPION@HP, showing a loading efficiency of 66.9 ± 2.7% and controlled release up to 120 h without any initial burst effect. Additionally, MTT assay revealed that DOX-loaded SPION@HP exerted great anticancer effect against HeLa cells and could be safely used. These results pave the way for the application of SPION@HP as an effective targeted delivery system for cancer treatment. 
546 |a EN 
690 |a iron oxide nanoparticles 
690 |a core-shell structure 
690 |a surface modification 
690 |a Poloxamer 
690 |a heparin 
690 |a doxorubicin 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 11, Iss 3, p 120 (2019) 
787 0 |n http://www.mdpi.com/1999-4923/11/3/120 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/f0b48e53b1bd4bb5a19a04fdffeaa1dd  |z Connect to this object online.